Variant #0000300344 (NC_000003.11:g.132441268T>C, NM_153240.4:c.-69A>G (NPHP3))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.132441268T>C
DNA change (hg38) g.132722424T>C
Published as NPHP3(NM_153240.5):c.-69A>G, NPHP3-ACAD11(NR_037804.1):n.36A>G
ISCN -
DB-ID NPHP3_000049
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UBA5 NM_024818.3 -/. - c.*45898T>C r.(=) p.(=)
ACAD11 NM_032169.4 -/. - c.-62673A>G r.(?) p.(=)
NPHP3 NM_153240.4 -/. - c.-69A>G r.(?) p.(=)
NPHP3-AS1 NR_002811.1 -/. - n.38+45T>C r.(?) -
NPHP3-ACAD11 NR_037804.1 -/. - n.36A>G r.(?) -


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